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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137736copy number variation1nstd102humanPathogenic GRCh37 chrX: 153,263,517-155,260,560 , GRCh38.p12 chrX: 153,998,066-156,030,895 H2AB3, GDI1, 83 more genes
    nsv6137735copy number variation1nstd102humanPathogenic GRCh37 chrX: 153,194,251-153,623,000 , GRCh38.p12 chrX: 153,928,798-154,394,658 EMD, MIR3202-1, 20 more genes
    nsv6112690copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301 LOC105373176, ZFX-AS1, 2151 more genes
    nsv5980455copy number variation1nstd102humanPathogenic GRCh38 chrX: 153,884,414-154,363,935 , GRCh37.p13 chrX|NW_003871103.3: 1,318,396-1,797,914 , GRCh37.p13 chrX: 153,149,868-153,592,303 MIR3202-1, FLNA, 23 more genes
    nsv5980392copy number variation1nstd102humanLikely pathogenic GRCh37 chrX: 153,296,033-153,296,163 , GRCh38 chrX: 154,030,582-154,030,712 MECP2
    nsv5674191copy number variation1nstd102humanPathogenic GRCh37 chrX: 153,357,622-153,363,142 , GRCh38.p12 chrX: 154,092,164-154,097,685 MECP2
    nsv5674190copy number variation1nstd102humanPathogenic GRCh37 chrX: 153,292,375-153,296,122 , GRCh38.p12 chrX: 154,026,924-154,030,671 MECP2
    nsv5673900copy number variation1nstd102humanPathogenic GRCh38 chrX: 154,030,637-154,038,771 , GRCh37 chrX: 153,296,088-153,304,222 MECP2
    nsv5673835copy number variation1nstd102humanPathogenic GRCh37 chrX: 153,128,098-153,498,669 , GRCh38.p12 chrX: 153,862,643-154,233,200 OPN1MW, IRAK1, 18 more genes
    nsv5564517copy number variation1nstd102humanPathogenic GRCh38 chrX: 153,858,452-154,332,213 , GRCh37.p13 chrX|NW_003871103.3: 1,292,435-1,766,192 , GRCh37.p13 chrX: 153,123,907-153,560,563 OPN1MW2, ARHGAP4, 22 more genes
    nsv5380359translocation1nstd200human GRCh38 chrX: 154,038,103-154,038,103 , GRCh38 chrX: 154,038,262-154,038,262 , GRCh37.p13 chrX|NW_003871103.3: 1,472,241-1,472,241 , GRCh37.p13 chrX: 153,303,713-153,303,713 , GRCh37.p13 chrX|NW_003871103.3: 1,472,082-1,472,082 , GRCh37.p13 chrX: 153,303,554-153,303,554 MECP2
    nsv5200320copy number variation1nstd102humanLikely pathogenic GRCh37 chrX: 153,296,044-153,303,808 , GRCh38 chrX: 154,030,593-154,038,357 MECP2
    nsv5200193mobile element insertion1nstd203human GRCh38 chrX: 154,088,984-154,088,986 , GRCh37.p13 chrX: 153,354,437-153,354,440 , GRCh37.p13 chrX|NW_003871103.3: 1,522,963-1,522,965 MECP2
    nsv5200192mobile element insertion1nstd203human GRCh38 chrX: 154,038,442-154,038,455 , GRCh37.p13 chrX|NW_003871103.3: 1,472,421-1,472,434 , GRCh37.p13 chrX: 153,303,893-153,303,906 MECP2
    nsv5060010copy number variation1nstd102humanPathogenic GRCh37 chrX: 153,296,228-153,298,081 , GRCh38 chrX: 154,030,777-154,032,630 MECP2
    nsv5059979copy number variation1nstd102humanPathogenic GRCh37 chrX: 56,469,080-155,233,731 , GRCh38.p12 chrX: 56,442,647-156,004,066 VDAC1P1, LOC105373299, 1364 more genes
    nsv4787970copy number variation1nstd200human GRCh37 chrX: 153,302,367-153,303,830 , GRCh38.p12 chrX: 154,036,916-154,038,379 MECP2
    nsv4769340copy number variation1nstd102humanPathogenic GRCh37 chrX: 153,296,111-153,302,495 , GRCh38 chrX: 154,030,660-154,037,044 MECP2
    nsv4769327copy number variation1nstd102humanPathogenic GRCh38 chrX: 154,030,668-154,039,637 , GRCh37 chrX: 153,296,119-153,305,088 MECP2
    nsv4769267copy number variation1nstd102humanPathogenic GRCh37 chrX: 153,296,038-153,299,936 , GRCh38 chrX: 154,030,587-154,034,485 MECP2
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